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Author Topic: Tips for beginning in-center hemo  (Read 3131 times)
kickingandscreaming
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« on: November 27, 2015, 03:30:57 PM »

Tomorrow I have my first in-center hemo treatment.  I am a nubie to the whole business.  I tried to do PD but my catheter won't work. Then I was in the hospital and they gave me a chest catheter for (urgent) hemo while there.  Now I am due tomorrow for hemo at a dialysis clinic until such time as my PD catheter gets sorted.  I'm looking for advice as to how to make the experience less awful than I imagine it to be.  I'm taking my laptop, but not sure if they have wifi or not.  Hate TV. Should I bring food? special clothing? What?  Thanks.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
Simon Dog
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« Reply #1 on: November 27, 2015, 03:52:52 PM »

Bring blanket, snacks and bottle of water.

Bring a laptop.    Internet may not work and, if it does, may not stream video.   Pay $40 for www.playlater.tv to pre-record Netflix, Hulu, etc. before the clinic visit.

Visit a Redbox on the way to a clinic.

Invest in high quality headphones.   I like the Bose.

If the headphones require batteries, bring spares.

Set up the Tor browser in case you want to visit any censored web sites from the clinic (FMC bans lots of legit, non-porn, web sites as politically unapproved).   VPN software also solves this problem.

Have a plan with you MD for home hemo if home PD does not work out for you.  It may help you stay sane while in the clinic.

Learn how fluid management works so you can make sure the tech or RN takes off the right amount.

If you don't like the amount of water being taken off and the tech won't change it, ask for the RN.    Techs have a lot less discretion as to machine settings.
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Michael Murphy
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« Reply #2 on: November 27, 2015, 04:07:55 PM »

Simon Dog provides a almost complete list of things to have for a dialysis session.  The two things Inrecommend most is too late for you now, have a fistula installed early so it can mature prior to dialysis second tour the center to learn what will happen when you go.  While it's too late for you maybe some one else about to start will read this.  However the most important thing beside the need to fill in the hours while you sit waiting for the session to end, is that the fear of what is going to happen is much worse than the actual event.  My first session was a nightmare not because of the actual dialysis but thr almost paralyising fear I had before going.  So relax its not as much fun as wining the lottery but it's a lot better then what you think,it's going to be.  The only thing else is you made need a cushion to sit on since the chairs are hard on some peoples butt and a blanket in case it's cold. Good luck.
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kickingandscreaming
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« Reply #3 on: November 27, 2015, 04:29:44 PM »

Thank you both.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
Simon Dog
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« Reply #4 on: November 27, 2015, 09:41:57 PM »

Quote
The only thing else is you made need a cushion to sit on since the chairs are hard on some peoples butt and a blanket in case it's cold. Good luck.
walmart.com - Drive brand wheelchair cushion
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Michael Murphy
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« Reply #5 on: November 28, 2015, 07:34:58 AM »

Just saw your quote about really living, I spend about 18 hours a week on dialysis, set up, treatment, holding.  There are 168 hours in a week, that leaves 150 hours to have a life.  I know it's not a great way to spend 18 hours, but most people with a life threatening disease would gladly spend the time to continue living.  Dialysis clearly sucks bur it's better then dead.
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kitkatz
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« Reply #6 on: November 28, 2015, 09:19:18 AM »

I look like I am running away from home when I go into my nocturnal dialysis.  I have lots of stuff with me in my bags.
I have two bags I carry in.  One is a huge IKEA blue bag- It has my chair bag stuff in it.  The other is a lunch type bag.


The Chair Bag Stuff
Twin size foam egg crate mattress- to help with the chair comfort. Can find it at Walmart for under 10.
Twin sheet folded in half to put over the foam mattress
Pillow with pillow case
Neck pillow
Large, queen size soft blanket folded in half.  Centers are known to be cold.
Extra change of clothes: Mumu, underwear, socks
Plastic bag for dirty clothes
Wipes

The Snack Bag
Ziploc bags are great for carrying snacks.I usually have two snacks in the bag each session, maybe three.
It is usually better not to eat an entire meal while at dialysis.  It can affect your blood pressure.
I find I sometimes am hungry, other nights  not interested in the snacks.
A good pair of noise blacking headphones- dialysis centers are NOISY, machines noises, other patients noises, and staff noise.
Kindle Fire Tablet- pre-download a few apps and books so you do not have too wait at the center to play or read.
Skier hand warmer pack to help with cold.
I also carry a large cup of ice with me.  It helps throughout the night because you are stuck there in a chair and cannot just get up for a drink and staff will usually not bring you a drink.


I have tummy trouble because of intestinal surgery, so before dialysis I take 2 Immodium. 
I also take 2 Tylenol about an hour before I go in.
I am also taking 2 Ambien for anxiety about 15 minutes before I arrive.






« Last Edit: November 28, 2015, 09:22:47 AM by kitkatz » Logged



lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
kickingandscreaming
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« Reply #7 on: November 28, 2015, 03:05:02 PM »

Thanks for the tips. I survived my first in-center dialysis.   I wasn't cold at all.  I brought my laptop and read and caught up with work  The nurses were very nice and attentive.  It IS noisy-- all those machines beeping all the time. I found it quite bright in there and think I will bring an eye mask so I can avoid all the fluorescent lights and maybe catch a couple of winks. I was able to drive myself home and that felt good.  There was absolutely no schmoozing among the patients which surprised me but was fine--as i'm not that social. The next few months until I get my PD catheter sorted will be pretty wild (not in the way I would prefer "wild.")
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
cassandra
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When all else fails run in circles, shout loudly

« Reply #8 on: November 28, 2015, 03:14:39 PM »

Real glad to read you'll be okay till PD time

      :cuddle;

Love, Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
kitkatz
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« Reply #9 on: November 28, 2015, 03:59:18 PM »

So glad to hear you did well the first time around.  Sunglasses may work to cut down the glare in center, too.
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
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